chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1234536549234536550T-25GENIChomozygous759222293
1234537237234537238GA21GENIChomozygous653627880
1234537481234537482GA30GENIChomozygous653627881
1234538935234538936AG28GENIChomozygous653627882
1234540396234540397GA26GENICpossibly homozygous653627883
1234540873234540874GC31GENIChomozygous653627884
1234541348234541349AC17GENIChomozygous653627885
1234541525234541526CT19GENIChomozygous653627886
1234541593234541594AG25GENIChomozygous653627887
1234541675234541676T-22GENIChomozygous759222294
1234541919234541920CT33GENIChomozygous653627888
1234542176234542190TCTCTCTCTCTCTT--------------9GENICheterozygous759222295
1234542845234542846TC33GENIChomozygous653627889
1234543307234543308C-28GENIChomozygous759222296
1234543884234543885CT26GENICpossibly homozygous653627890
1234545140234545144CTTC----19GENIChomozygous759222297
1234545145234545148AAT---18GENIChomozygous759222298
1234545829234545830G-18GENIChomozygous759222299
1234546078234546079CCAAAAAAA8GENICheterozygous759222303
1234546453234546454GA28GENIChomozygous653627891
1234547466234547467T-19GENICpossibly homozygous759222304
1234547535234547536GA17GENICpossibly homozygous653627892
1234548632234548633GA19GENIChomozygous653627893
1234549211234549212CG19GENIChomozygous653627894
1234549900234549901TC33GENIChomozygous653627895
1234550819234550820AG30GENIChomozygous653627896
1234551113234551114CA26GENIChomozygous653627897
1234551415234551416GA26GENIChomozygous653627898
1234551418234551419TG27GENIChomozygous653627899